氧化还原
材料科学
磁滞
电池(电)
电压
电极
化学工程
光电子学
无机化学
纳米技术
电气工程
功率(物理)
物理化学
化学
热力学
凝聚态物理
物理
工程类
冶金
作者
Kehua Dai,Jing Mao,Zengqing Zhuo,Yan Feng,Wenfeng Mao,Guo Ai,Feng Pan,Yi‐De Chuang,Gao Liu,Wanli Yang
出处
期刊:Nano Energy
[Elsevier BV]
日期:2020-04-25
卷期号:74: 104831-104831
被引量:118
标识
DOI:10.1016/j.nanoen.2020.104831
摘要
Lattice anionic (oxygen) redox reactions (ARR) offers opportunities for developing high-capacity batteries, however, often suffers the notoriously high hysteresis in voltages and low initial coulombic efficiency. Particularly, ARR was widely considered inherent to these kinetic issues. In this paper, unambiguous evidences of strong and reversible ARR is found in Na2/3Ni1/3Mn2/3O2 through mapping of resonant inelastic X-ray scattering (mRIXS). Strikingly, the material displays negligible voltage hysteresis (0.1 V) and high initial coulombic efficiency with a highly stable electrochemical profile. Our independent analysis of the Ni, Mn and O states consistently interpret the redox mechanism of Na2/3Ni1/3Mn2/3O2, which reveals a strong ARR system with facile kinetics and highly stable electrochemical profile that previously found only in cationic redox systems of conventional non-Alkali-rich materials.
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